A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197797



Internal ID20764837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:360195..506451hg38UCSC Ensembl
chr19:360195..506451hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38146257
hg19146257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534360
Supporting Variants
Samples
Known GenesC2CD4C, MADCAM1, ODF3L2, SHC2, THEG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer